Chapter 18: Problem 29
Treating choline with acetic anhydride gives acetylcholine, a neurotransmitter. Write an equation for the formation of acetylcholine. $$ \left(\mathrm{CH}_{3}\right)_{3} \mathrm{NCH}_{2} \mathrm{CH}_{2} \mathrm{OH} $$ Choline
Chapter 18: Problem 29
Treating choline with acetic anhydride gives acetylcholine, a neurotransmitter. Write an equation for the formation of acetylcholine. $$ \left(\mathrm{CH}_{3}\right)_{3} \mathrm{NCH}_{2} \mathrm{CH}_{2} \mathrm{OH} $$ Choline
All the tools & learning materials you need for study success - in one app.
Get started for freeUsing your roadmaps as a guide, show how to convert 1-bromopentane and sodium cyanide into \(N\)-hexylhexanamide. You must use 1-bromopentane and sodium cyanide as the source of all carbon atoms in the target molecule. Show all reagents and all molecules synthesized along the way.
The mechanism for hydrolysis of an ester in aqueous acid involves formation of a tetrahedral carbonyl addition intermediate. Evidence in support of this mechanism comes from an experiment designed by Myron Bender. He first prepared ethyl benzoate enriched with oxygen-18 in the carbonyl oxygen and then carried out acid-catalyzed hydrolysis of the ester in water containing no enrichment in oxygen-18. If he stopped the experiment after only partial hydrolysis and isolated the remaining ester, the recovered ethyl benzoate lost a portion of its enrichment in oxygen-18. In other words, some exchange had occurred between oxygen-18 of the ester and oxygen-16 of water. Show how this observation bears on the formation of a tetrahedral carbonyl addition intermediate during acid-catalyzed ester hydrolysis.
Following is a retrosynthetic analysis for the synthesis of the herbicide (S)-Metolachlor from 2-ethyl-6-methylaniline, chloroacetic acid, acetone, and methanol. Show reagents and experimental conditions for the synthesis of Metolachlor from these four organic starting materials. Your synthesis will most likely give a racemic mixture. The chiral catalyst used by Novartis for reduction in Step 2 gives \(80 \%\) enantiomeric excess of the \(S\) enantiomer.
Reaction of a primary or secondary amine with diethyl carbonate under
controlled conditions gives a carbamic ester.
Complete the following transesterification reaction (the stoichiometry is given in the equation).
What do you think about this solution?
We value your feedback to improve our textbook solutions.